4.8 Article

Channelopathies: Kir2.1 mutations jeopardize many cell functions

Journal

CURRENT BIOLOGY
Volume 11, Issue 18, Pages R747-R750

Publisher

CELL PRESS
DOI: 10.1016/S0960-9822(01)00437-7

Keywords

-

Ask authors/readers for more resources

Andersen's syndrome is caused by mutations in the potassium channel Kir2.1, a major determinant of resting membrane potential. The clinical features of this disease illustrate the importance of a stable resting membrane potential for many cell functions.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available